Objective. Students will insert a supraglottic airway device (including laryngeal mask airway and King LT or equivalent, per program equipment) into an adult airway manikin, confirm placement, and identify clinical situations in which a supraglottic device is preferred over endotracheal intubation.
This lesson, its worked examples and its practice questions has not yet been verified by a licensed clinician in the field or by a certification or approval body. It is a study draft and may contain errors. Do not use it to make decisions about any patient or medication. Always follow your instructor, your supervising professional, and current official references and regulations.
VoTechWorks program approval and accreditation are still in progress. Credentials are issued only by the certifying bodies named in each program, after their own exams.
Supraglottic airway devices (SGAs) are airway adjuncts that are inserted into the oropharynx or hypopharynx and sit above (supra) the glottic opening. Unlike an endotracheal tube (ETT), which passes through the vocal cords into the trachea, an SGA creates a seal around or near the laryngeal inlet without entering the trachea. This design makes insertion faster to learn, faster to perform, and less technically demanding than endotracheal intubation — advantages that matter greatly in the prehospital setting.
Common SGA types used in EMS include the Laryngeal Mask Airway (LMA), the King LT (Laryngeal Tube), and the i-gel. Each works by a slightly different mechanism, but all allow ventilation via a bag-valve mask (BVM) without direct visualization of the cords.
Laryngeal Mask Airway (LMA): The LMA has an elliptical mask at its distal end. When inserted and inflated, the mask seals around the laryngeal inlet, allowing positive-pressure ventilation. It does not protect against aspiration as completely as a cuffed ETT. Standard LMAs come in numbered sizes based on patient weight.
King LT (Laryngeal Tube): The King LT is a dual-lumen, dual-cuff tube. The distal cuff seals the esophagus; the proximal cuff seals the oropharynx. Ventilation occurs through the port between the two cuffs, which sits at the level of the larynx. Both cuffs are inflated with a single syringe through one inflation port, with the volume determined by the color-coded size of the device. Sizes are selected based on patient height.
i-gel: The i-gel uses a soft, non-inflatable thermoplastic gel cuff that conforms to the perilaryngeal anatomy without active inflation. There are no cuff inflation steps, which simplifies insertion. Size is selected by patient weight.
Although specific steps vary by device, the general sequence for SGA insertion is:
1. Select the correct size using the manufacturer's size chart (weight or height depending on device).
2. Prepare the device — lubricate the cuff or distal tip with water-soluble lubricant; for cuff-based devices, fully deflate the cuff before insertion.
3. Position the patient — sniffing position (slight head extension, neck flexion) or neutral position if spinal precautions are needed.
4. Insert the device — follow the natural curve of the airway; advance until resistance is felt or the manufacturer's depth marking is reached.
5. Inflate the cuff — inject the volume specified for that device size (King LT and LMA only; not applicable for i-gel).
6. Attach BVM and ventilate — deliver a breath while watching for bilateral chest rise.
7. Confirm placement — auscultate bilateral breath sounds in the midaxillary lines and absence of epigastric sounds. Use waveform capnography if available, as it is the gold standard for confirming ventilation.
8. Secure the device and continue monitoring.
SGAs are generally preferred or indicated when:
SGAs are generally not preferred when: the patient has an intact gag reflex; there is a known or suspected airway obstruction below the glottis; the patient requires very high ventilation pressures (e.g., severe bronchospasm) that may exceed the device's seal pressure; or local protocol mandates ETI as the primary advanced airway.
Waveform capnography provides continuous, quantitative confirmation that ventilation is occurring. A flat waveform after SGA insertion means either the device is misplaced, the airway is obstructed, or the patient has no cardiac output — each requiring immediate action. Never rely on chest rise alone as the sole confirmation method.
Answer each question, then check it. Nothing is recorded; this is your own practice.
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